The clinical phenotype of autosomal dominant lateral temporal lobe epilepsy related to reelin mutations
Michelucci, Roberto, Pulitano, Patrizia, Di Bonaventura, Carlo, Binelli, Simona, Luisi, Concetta, Pasini, Elena, Striano, Salvatore, Striano, Pasquale, Coppola, Giangennaro, La Neve, Angela, Giallonardo, Anna Teresa, Mecarelli, Oriano, Serioli, Elena, Dazzo, Emanuela, Fanciulli, Manuela, Nobile, Carlo
Published in Epilepsy & behavior (01.03.2017)
Published in Epilepsy & behavior (01.03.2017)
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Ocular refraction: heritability and genome-wide search for eye morphometry traits in an isolated Sardinian population
BIINO, Ginevra, PALMAS, Maria Antonietta, CORONA, Carla, PRODI, Dionigio, FANCIULLI, Manuela, SULIS, Roberta, SERRA, Antonina, FOSSARELLO, Maurizio, PIRASTU, Mario
Published in Human genetics (01.02.2005)
Published in Human genetics (01.02.2005)
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Journal Article
Microsatellites and SNPs linkage analysis in a Sardinian genetic isolate confirms several essential hypertension loci previously identified in different populations
Mocci, Evelina, Concas, Maria P, Fanciulli, Manuela, Pirastu, Nicola, Adamo, Mauro, Cabras, Valentina, Fraumene, Cristina, Persico, Ivana, Sassu, Alessandro, Picciau, Andrea, Prodi, Dionigio A, Serra, Donatella, Biino, Ginevra, Pirastu, Mario, Angius, Andrea
Published in BMC medical genetics (28.08.2009)
Published in BMC medical genetics (28.08.2009)
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Journal Article
FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity
Aitman, Timothy J, Fanciulli, Manuela, Norsworthy, Penny J, Petretto, Enrico, Dong, Rong, Harper, Lorraine, Kamesh, Lavanya, Heward, Joanne M, Gough, Stephen C L, de Smith, Adam, Blakemore, Alexandra I F, Froguel, Philippe, Owen, Catherine J, Pearce, Simon H S, Teixeira, Luis, Guillevin, Loic, Graham, Deborah S Cunninghame, Pusey, Charles D, Cook, H Terence, Vyse, Timothy J
Published in Nature genetics (01.06.2007)
Published in Nature genetics (01.06.2007)
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Journal Article
Copy number variations and susceptibility to lateral temporal epilepsy: A study of 21 pedigrees
Fanciulli, Manuela, Pasini, Elena, Malacrida, Sandro, Striano, Pasquale, Striano, Salvatore, Michelucci, Roberto, Ottman, Ruth, Nobile, Carlo
Published in Epilepsia (Copenhagen) (01.10.2014)
Published in Epilepsia (Copenhagen) (01.10.2014)
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Journal Article
Suggestive linkage of familial mesial temporal lobe epilepsy to chromosome 3q26
Fanciulli, Manuela, Di Bonaventura, Carlo, Egeo, Gabriella, Fattouch, Jinane, Dazzo, Emanuela, Radovic, Slobodanka, Spadotto, Alessandro, Giallonardo, Anna Teresa, Nobile, Carlo
Published in Epilepsy research (01.02.2014)
Published in Epilepsy research (01.02.2014)
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Identification of a PKP2 gene deletion in a family with arrhythmogenic right ventricular cardiomyopathy
Li Mura, Ilena Egle Astrid, Bauce, Barbara, Nava, Andrea, Fanciulli, Manuela, Vazza, Giovanni, Mazzotti, Elisa, Rigato, Ilaria, De Bortoli, Marzia, Beffagna, Giorgia, Lorenzon, Alessandra, Calore, Martina, Dazzo, Emanuela, Nobile, Carlo, Mostacciuolo, Maria Luisa, Corrado, Domenico, Basso, Cristina, Daliento, Luciano, Thiene, Gaetano, Rampazzo, Alessandra
Published in European journal of human genetics : EJHG (01.11.2013)
Published in European journal of human genetics : EJHG (01.11.2013)
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Journal Article
Heterozygous Reelin Mutations Cause Autosomal-Dominant Lateral Temporal Epilepsy
Dazzo, Emanuela, Fanciulli, Manuela, Serioli, Elena, Minervini, Giovanni, Pulitano, Patrizia, Binelli, Simona, Di Bonaventura, Carlo, Luisi, Concetta, Pasini, Elena, Striano, Salvatore, Striano, Pasquale, Coppola, Giangennaro, Chiavegato, Angela, Radovic, Slobodanka, Spadotto, Alessandro, Uzzau, Sergio, La Neve, Angela, Giallonardo, Anna Teresa, Mecarelli, Oriano, Tosatto, Silvio C.E., Ottman, Ruth, Michelucci, Roberto, Nobile, Carlo
Published in American journal of human genetics (04.06.2015)
Published in American journal of human genetics (04.06.2015)
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Journal Article
Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutations
Michelucci, Roberto, Pasini, Elena, Malacrida, Sandro, Striano, Pasquale, Bonaventura, Carlo Di, Pulitano, Patrizia, Bisulli, Francesca, Egeo, Gabriella, Santulli, Lia, Sofia, Vito, Gambardella, Antonio, Elia, Maurizio, Falco, Arturo, Neve, Angela la, Banfi, Paola, Coppola, Giangennaro, Avoni, Patrizia, Binelli, Simona, Boniver, Clementina, Pisano, Tiziana, Marchini, Marco, Dazzo, Emanuela, Fanciulli, Manuela, Bartolini, Yerma, Riguzzi, Patrizia, Volpi, Lilia, Falco, Fabrizio A., Giallonardo, Anna Teresa, Mecarelli, Oriano, Striano, Salvatore, Tinuper, Paolo, Nobile, Carlo
Published in Epilepsia (Copenhagen) (01.07.2013)
Published in Epilepsia (Copenhagen) (01.07.2013)
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Journal Article
Molecular changes induced by the curcumin analogue D6 in human melanoma cells
Rozzo, Carla, Fanciulli, Manuela, Fraumene, Cristina, Corrias, Antonio, Cubeddu, Tiziana, Sassu, Ilaria, Cossu, Sara, Nieddu, Valentina, Galleri, Grazia, Azara, Emanuela, Dettori, Maria Antonietta, Fabbri, Davide, Palmieri, Giuseppe, Pisano, Marina
Published in Molecular cancer (04.05.2013)
Published in Molecular cancer (04.05.2013)
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Journal Article
Association of variation in Fcγ receptor 3B gene copy number with rheumatoid arthritis in Caucasian samples
McKinney, Cushla, Fanciulli, Manuela, Merriman, Marilyn E, Phipps-Green, Amanda, Alizadeh, Behrooz Z, Koeleman, Bobby P C, Dalbeth, Nicola, Gow, Peter J, Harrison, Andrew A, Highton, John, Jones, Peter B, Stamp, Lisa K, Steer, Sophia, Barrera, Pilar, Coenen, Marieke J H, Franke, Barbara, van Riel, Piet L C M, Vyse, Tim J, Aitman, Tim J, Radstake, Timothy R D J, Merriman, Tony R
Published in Annals of the rheumatic diseases (01.09.2010)
Published in Annals of the rheumatic diseases (01.09.2010)
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Journal Article
FCGR3B copy number variation is associated with systemic lupus erythematosus risk in Afro-Caribbeans
Molokhia, Mariam, Fanciulli, Manuela, Petretto, Enrico, Patrick, Alan Leslie, McKeigue, Paul, Roberts, Amy L., Vyse, Tim J., Aitman, Tim J.
Published in Rheumatology (Oxford, England) (01.07.2011)
Published in Rheumatology (Oxford, England) (01.07.2011)
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Journal Article
Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI 1 mutations
Michelucci, Roberto, Pasini, Elena, Malacrida, Sandro, Striano, Pasquale, Bonaventura, Carlo Di, Pulitano, Patrizia, Bisulli, Francesca, Egeo, Gabriella, Santulli, Lia, Sofia, Vito, Gambardella, Antonio, Elia, Maurizio, de Falco, Arturo, Neve, Angela la, Banfi, Paola, Coppola, Giangennaro, Avoni, Patrizia, Binelli, Simona, Boniver, Clementina, Pisano, Tiziana, Marchini, Marco, Dazzo, Emanuela, Fanciulli, Manuela, Bartolini, Yerma, Riguzzi, Patrizia, Volpi, Lilia, de Falco, Fabrizio A., Giallonardo, Anna Teresa, Mecarelli, Oriano, Striano, Salvatore, Tinuper, Paolo, Nobile, Carlo
Published in Epilepsia (Copenhagen) (01.07.2013)
Published in Epilepsia (Copenhagen) (01.07.2013)
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Journal Article
A New Essential Hypertension Susceptibility Locus on Chromosome 2p24-p25, Detected by Genomewide Search
Angius, Andrea, Petretto, Enrico, Maestrale, Giovanni Battista, Forabosco, Paola, Casu, Giuseppina, Piras, Daniela, Fanciulli, Manuela, Falchi, Mario, Melis, Paola Maria, Palermo, Mario, Pirastu, Mario
Published in American journal of human genetics (01.10.2002)
Published in American journal of human genetics (01.10.2002)
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Journal Article
Association of variation in Fcg receptor 3B gene copy number with rheumatoid arthritis in Caucasian samples
McKinney, Cushla, Fanciulli, Manuela, Merriman, Marilyn E, Phipps-Green, Amanda, Alizadeh, Behrooz Z, Koeleman, Bobby P C, Dalbeth, Nicola, Gow, Peter J, Harrison, Andrew A, Highton, John, Jones, Peter B, Stamp, Lisa K, Steer, Sophia, Barrera, Pilar, Coenen, Marieke J H, Franke, Barbara, van Riel, Piet L C M, Vyse, Tim J, Aitman, Tim J, Radstake, Timothy R D J, Merriman, Tony R
Published in Annals of the rheumatic diseases (01.09.2010)
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Published in Annals of the rheumatic diseases (01.09.2010)
Journal Article
Association of variation in Fc receptor 3B gene copy number with rheumatoid arthritis in Caucasian samples
McKinney, C., Fanciulli, M., Merriman, M. E., Phipps-Green, A., Alizadeh, B. Z., Koeleman, B. P. C., Dalbeth, N., Gow, P. J., Harrison, A. A., Highton, J., Jones, P. B., Stamp, L. K., Steer, S., Barrera, P., Coenen, M. J. H., Franke, B., van Riel, P. L. C. M., Vyse, T. J., Aitman, T. J., Radstake, T. R. D. J., Merriman, T. R.
Published in Annals of the rheumatic diseases (01.09.2010)
Published in Annals of the rheumatic diseases (01.09.2010)
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Journal Article
FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity
FANCIULLI, Manuela, NORSWORTHY, Penny J, FROGUEL, Philippe, OWEN, Catherine J, PEARCE, Simon H. S, TEIXEIRA, Luis, GUILLEVIN, Loic, GRAHAM, Deborah S. Cunninghame, PUSEY, Charles D, COOK, H. Terence, VYSE, Timothy J, AITMAN, Timothy J, PETRETTO, Enrico, RONG DONG, HARPER, Lorraine, KAMESH, Lavanya, HEWARD, Joanne M, GOUGH, Stephen C. L, DE SMITH, Adam, BLAKEMORE, Alexandra F
Published in Nature genetics (2007)
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Published in Nature genetics (2007)
Journal Article
Association of variation in Fcgamma receptor 3B gene copy number with rheumatoid arthritis in Caucasian samples
McKinney, Cushla, Fanciulli, Manuela, Merriman, Marilyn E, Phipps-Green, Amanda, Alizadeh, Behrooz Z, Koeleman, Bobby P C, Dalbeth, Nicola, Gow, Peter J, Harrison, Andrew A, Highton, John, Jones, Peter B, Stamp, Lisa K, Steer, Sophia, Barrera, Pilar, Coenen, Marieke J H, Franke, Barbara, van Riel, Piet L C M, Vyse, Tim J, Aitman, Tim J, Radstake, Timothy R D J, Merriman, Tony R
Published in Annals of the rheumatic diseases (01.09.2010)
Published in Annals of the rheumatic diseases (01.09.2010)
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Journal Article